Matches in Nanopublications for { ?s ?p "[Loss-of-function mutations of the MECP2 gene are the cause of most cases of Rett syndrome in females, a progressive neurodevelopmental disorder characterized by severe mental retardation, global regression, hand stereotypies, and microcephaly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP206472.RAjX5nHYTfBlaIDQcHSojFcjpGuygZ7sR9RJdxIVGfnPs130_assertion description "[Loss-of-function mutations of the MECP2 gene are the cause of most cases of Rett syndrome in females, a progressive neurodevelopmental disorder characterized by severe mental retardation, global regression, hand stereotypies, and microcephaly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP206472.RAjX5nHYTfBlaIDQcHSojFcjpGuygZ7sR9RJdxIVGfnPs130_provenance.
- NP448785.RAgXZEqLRKrrb4cAyoR7Bxequpfg-iIOVxhdHFJEzrZvA130_assertion description "[Loss-of-function mutations of the MECP2 gene are the cause of most cases of Rett syndrome in females, a progressive neurodevelopmental disorder characterized by severe mental retardation, global regression, hand stereotypies, and microcephaly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP448785.RAgXZEqLRKrrb4cAyoR7Bxequpfg-iIOVxhdHFJEzrZvA130_provenance.
- NP925211.RA17SvFCdwl33ZRCSqxn5tkDlt0XB2TGYUQGMxceJXH0Y130_assertion description "[Loss-of-function mutations of the MECP2 gene are the cause of most cases of Rett syndrome in females, a progressive neurodevelopmental disorder characterized by severe mental retardation, global regression, hand stereotypies, and microcephaly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP925211.RA17SvFCdwl33ZRCSqxn5tkDlt0XB2TGYUQGMxceJXH0Y130_provenance.
- NP551935.RAHVZvCg-0VILNdyRwF9lkIcL6uCxEFs_IyYXR3dJiwoo130_assertion description "[Loss-of-function mutations of the MECP2 gene are the cause of most cases of Rett syndrome in females, a progressive neurodevelopmental disorder characterized by severe mental retardation, global regression, hand stereotypies, and microcephaly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP551935.RAHVZvCg-0VILNdyRwF9lkIcL6uCxEFs_IyYXR3dJiwoo130_provenance.
- assertion description "[Loss-of-function mutations of the MECP2 gene are the cause of most cases of Rett syndrome in females, a progressive neurodevelopmental disorder characterized by severe mental retardation, global regression, hand stereotypies, and microcephaly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP925212.RAl-HlsD3iIeSrgyDIY4mamGvjU9kszjneV5cmv0mjMT0130_assertion description "[Loss-of-function mutations of the MECP2 gene are the cause of most cases of Rett syndrome in females, a progressive neurodevelopmental disorder characterized by severe mental retardation, global regression, hand stereotypies, and microcephaly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP925212.RAl-HlsD3iIeSrgyDIY4mamGvjU9kszjneV5cmv0mjMT0130_provenance.